| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6619375-6619607 | Common:6; Rare:130; Clinvar:4; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
| chr11:6683255-6683637 | Common:12; Rare:283 | ||||
| chr11:7513632-7514098 | Common:11; Rare:258 | ||||
| chr11:7573764-7573993 | Rare:72 | ||||
| chr11:7673487-7673591 | Common:1; Rare:38 | ||||
| chr11:8081076-8081343 | Common:6; Rare:145 | ||||
| chr11:8594133-8594401 | Common:2; Rare:133 | ||||
| chr11:8682611-8683036 | Common:4; Rare:310 | ||||
| chr11:8718021-8718182 | Common:6; Rare:34 | ||||
| chr11:8776236-8776901 | Common:3; Rare:144 | ||||
| chr11:8910912-8911266 | Common:6; Rare:97 | ||||
| chr11:8964376-8964591 | Common:6; Rare:130 | ||||
| chr11:8964700-8965140 | Common:3; Rare:140 | ||||
| chr11:9265283-9265483 | Rare:129 | ||||
| chr11:9314440-9314966 | Common:13; Rare:318 |